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在接受阿特珠单抗治疗的非小细胞肺癌患者中,对循环生物标志物的 PK/PD 分析及其与肿瘤应答的关系。

A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab-Treated non-small Cell Lung Cancer Patients.

机构信息

Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.

Pharmetheus AB, Uppsala, Sweden.

出版信息

Clin Pharmacol Ther. 2019 Feb;105(2):486-495. doi: 10.1002/cpt.1198. Epub 2018 Sep 4.

Abstract

To assess circulating biomarkers as predictors of antitumor response to atezolizumab (anti-programmed death-ligand 1 (PD-L1), Tecentriq) serum pharmacokinetic (PK) and 95 plasma biomarkers were analyzed in 88 patients with relapsed/refractory non-small cell lung cancer (NSCLC) receiving atezolizumab i.v. q3w (10-20 mg/kg) in the PCD4989g phase I clinical trial. Following exploratory analyses, two plasma biomarkers were chosen for further study and correlation with change in tumor size (the sum of the longest diameter) was assessed in a pharmacokinetic/pharmacodynamic (PK/PD) tumor modeling framework. When longitudinal kinetics of biomarkers and tumor size were modeled, tumor shrinkage was found to significantly correlate with area under the curve (AUC), baseline factors (metastatic sites, liver metastases, and smoking status), and relative change in interleukin (IL)-18 level from baseline at day 21 (RCFB ). Although AUC was a major predictor of tumor shrinkage, the effect was estimated to dissipate with an average half-life of 80 days, whereas RCFB seemed relevant to the duration of the response.

摘要

为了评估循环生物标志物作为抗 PD-L1(阿替利珠单抗,Tecentriq)治疗抗肿瘤反应的预测因子,对接受阿替利珠单抗静脉注射 q3w(10-20mg/kg)治疗的 88 例复发/难治性非小细胞肺癌(NSCLC)患者的 88 例患者的血清药代动力学(PK)和 95 种血浆生物标志物进行了分析。在探索性分析后,选择了两种血浆生物标志物进行进一步研究,并在 PK/PD 肿瘤建模框架中评估了它们与肿瘤大小变化的相关性。当对生物标志物和肿瘤大小的纵向动力学进行建模时,发现肿瘤缩小与曲线下面积(AUC)、基线因素(转移部位、肝转移和吸烟状态)以及 21 天(RCFB)时从基线水平的白细胞介素(IL)-18 水平的相对变化显著相关。尽管 AUC 是肿瘤缩小的主要预测因子,但据估计,其效应会随着平均半衰期为 80 天而消散,而 RCFB 似乎与反应持续时间相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c19/6704358/3c55117b660f/CPT-105-486-g001.jpg

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